US161137A - Improvement in processes of manufacturing ammonia - Google Patents
Improvement in processes of manufacturing ammonia Download PDFInfo
- Publication number
- US161137A US161137A US161137DA US161137A US 161137 A US161137 A US 161137A US 161137D A US161137D A US 161137DA US 161137 A US161137 A US 161137A
- Authority
- US
- United States
- Prior art keywords
- nitrogen
- improvement
- processes
- hydrogen
- alloy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen; Reversible storage of hydrogen
- C01B3/02—Production of hydrogen; Production of gaseous mixtures containing hydrogen
- C01B3/025—Preparation or purification of gas mixtures for ammonia synthesis
Definitions
- This said alloy is subjected to a moderate degree of heat in a closed chamber, and a mixture of nitrogen and hydrogen (or a hydrogen compound) is then passed over the alloy, which produces, under the influences of heat and chemical affinity, a combination of nitrogen and hydrogen to form ammonia.
- I produce, first of all, a combination or alloy of one of the more easily oxidizable metals (say, for instance, potassium, sodium, one of the alkalino-earthy metals, or even zinc) with one of the triad elements, as, for instance,
- Such an alloy may, for convenience, be produced by calcining oxide of antimony, or the powder or a suitable salt of that metal, with carbonate of soda or potassa, and enough charcoal or organic matter to eii'ect the reduction, or with any proper reducing material. If the carbon or organic matter be in sufficient excess, it retains the reduced metals in an amorphous and porous state, fit to be rapidly acted on in the subsequent treatment.
- Arsenide of sodium, phosphide of sodium, bismuthide of sodium, tin, and sodium produce similar results with nitrogen and aqueous vapornot all, however, to the same extent.
- the sodium may be here replaced by the other alkaline metals, alkalino earthy metals, or by nine, or by a mixture of them.
- M represents the triad or pentad element, and It the oxidizable metal
- N nitrogen
- H by drogen
- the presence of the triad or pentad element is essential to the process, but the presence of hydrogen in'the nascent form is also essential. ,7
- I may add that, in order to regenerate the metallic alloy or combination, and to reproduce the ammonia-producing compound, it is suflicient to expose the same to a red heat under the action of a reducing agent-gaseous, liquid, solid, inorganic, or organic; for instance, if enough carbon still remains in the compound, simple heating to redness will regenerate it.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Inorganic Chemistry (AREA)
- Solid-Phase Diffusion Into Metallic Material Surfaces (AREA)
Description
NH IJD "ME FARNHAM MAXWELL-Lycra, or PARIS, nnxnon.
IMPROVEMENT lN PROCESSES OF MANUFACTURING AMMONIA.
Specification forming part of Letters Patent No. [6 1,137, dated March 23, 1875; application filed March 10, 1875.
face.
This said alloy is subjected to a moderate degree of heat in a closed chamber, and a mixture of nitrogen and hydrogen (or a hydrogen compound) is then passed over the alloy, which produces, under the influences of heat and chemical affinity, a combination of nitrogen and hydrogen to form ammonia.
I produce, first of all, a combination or alloy of one of the more easily oxidizable metals (say, for instance, potassium, sodium, one of the alkalino-earthy metals, or even zinc) with one of the triad elements, as, for instance,
antimony, bismuth, arsenic, phosphorus, or
tin, it being understood that the combination or alloy in question should be of such chemical or physical constitution as to be able to decompose water or watery vapor at a moderate temperature, not exceeding that of low or incipient redness. An alloy of antimony and sodium or potassium, for instance, which decomposes water at ordinary temperatures, and rapidly at the boiling heat, is of this nature.
Such an alloy may, for convenience, be produced by calcining oxide of antimony, or the powder or a suitable salt of that metal, with carbonate of soda or potassa, and enough charcoal or organic matter to eii'ect the reduction, or with any proper reducing material. If the carbon or organic matter be in sufficient excess, it retains the reduced metals in an amorphous and porous state, fit to be rapidly acted on in the subsequent treatment.
I now place this reduced alloy or combination in a proper receptacle, and expose it to the action of a mixture of aqueous vapor and nitrogen, when the sodium or potassium of the alloy, uniting with the oxygen of the water, produces hydrogen, which, in its nascent state, combines with the nitrogen present, and produces ammonia.
Arsenide of sodium, phosphide of sodium, bismuthide of sodium, tin, and sodium produce similar results with nitrogen and aqueous vapornot all, however, to the same extent.
The process being accelerated by heat, it is advisable to maintain the material at a temperature of from 212 to 750 Fahrenheit during the passage of the nitrogen and aqueous vapor. The sodium may be here replaced by the other alkaline metals, alkalino earthy metals, or by nine, or by a mixture of them.
The reaction here employed may be represented by the following general formula, where M represents the triad or pentad element, and It the oxidizable metal; N, nitrogen; H, by drogen, and 0 oxygen: 2(MR )+2N+3(H O) =M +6(RO)+2(NH The presence of the triad or pentad element is essential to the process, but the presence of hydrogen in'the nascent form is also essential. ,7
I may add that, in order to regenerate the metallic alloy or combination, and to reproduce the ammonia-producing compound, it is suflicient to expose the same to a red heat under the action of a reducing agent-gaseous, liquid, solid, inorganic, or organic; for instance, if enough carbon still remains in the compound, simple heating to redness will regenerate it.
It is evident that in this reaction it may also be presumed that there is formation of a hydrogen compound of the triad or pentad, which is subsequently decomposed in contact with the nitrogen present, as, for instance, the compound of triad antimony with hydrogen. The reaction in this case would not be represented as above, and would be thus for the case of antimony: SbH +N=N 11 Sb, or, generally, MH +N=M+NH but in this case it is none the less certain that we have, equally as before, the presence of nascent hydrogen with nitrogen, and the simultaneous presence of a triad, which combination of substances A'rnN'r FIG,
forms the basis of the present patent, the presence of aqueous vapor being merely an accessory requisite for production of nascent hydrogen in certain cases.
I claim- The herein-described process of producing ammonia by the combination of nitrogen with nascent hydrogen liberated in the presence of a triad or pentad element, substantially as described.
FARNHAM MAXWELL-LYTE. Witnesses R0131. M. HOOPER, EMILE DUHAN.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US161137A true US161137A (en) | 1875-03-23 |
Family
ID=2230546
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US161137D Expired - Lifetime US161137A (en) | Improvement in processes of manufacturing ammonia |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US161137A (en) |
-
0
- US US161137D patent/US161137A/en not_active Expired - Lifetime
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US1519470A (en) | Impregnated carbon and process of making same | |
| Orhanovic et al. | Kinetic studies of the reactions of peroxy compounds of chromium (VI), vanadium (V), and titanium (IV) in acid media | |
| MacNeil et al. | Catalytic decomposition of ammonium nitrate in superheated aqueous solutions | |
| US3945919A (en) | Process for the environmentally favorable destruction of solid and/or liquid cyanide waste | |
| Poulston et al. | Surface redox characteristics of mixed oxide catalysts used for selective oxidation | |
| Dave et al. | Influence of BaZnCuO3 and BaZnCuO3/rGO on the thermal decomposition of ammonium perchlorate and 3‐nitro‐3H‐1, 2, 4‐triazol‐5‐one (NTO) | |
| KR102241757B1 (en) | Manufacturing method for platinum composite catalyst | |
| CN106881088A (en) | A kind of air oxidation broken cyanide catalyst and preparation method thereof | |
| US3502576A (en) | Process for detoxification of cyanide and nitrite containing aqueous solutions | |
| JP3314410B2 (en) | Method for treating cyanide | |
| WO1995004002A1 (en) | Treatment of cyanides in effluents with caro's acid | |
| US3336167A (en) | Process for treatment of surfaces of iron and steel | |
| US1992637A (en) | Production of nitroso compounds of cobalt | |
| Dhar | Action of nitric acid on metals | |
| US1359080A (en) | Process for the manufacture of alkaliamids | |
| Pesce | Cyanides | |
| US1239125A (en) | Process of oxidizing ammonia and catalytic bodies therefor. | |
| US374618A (en) | William fkederick hast | |
| JPS587357B2 (en) | cyanobunkaihouhou | |
| AT40719B (en) | Process for the preparation of ammonia. | |
| US1251204A (en) | Process of making catalyzers. | |
| US2683648A (en) | Process for purifying alkali metal cyanates | |
| US3486846A (en) | Process for the manufacture of hydroxyl-ammonium-salts | |
| US1166524A (en) | Process of purifying electrolytic chlorin. | |
| US899705A (en) | Method of production of nitrites. |